[NH2:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][CH:15]=1)[C:5]([C@H:7]1[CH2:9][C@H:8]1[C:10](O)=[O:11])=O.O.[NH2:17][NH2:18]>C(O)C>[NH2:1][C:2]1[CH:3]=[C:4]([C:5]2[CH:7]3[CH:8]([C:10](=[O:11])[NH:17][N:18]=2)[CH2:9]3)[CH:13]=[CH:14][CH:15]=1600 mg (2.9 millimoles) of cis-2-(m-aminobenzoyl)-cyclopropanecarboxylic acid, 20 ml of ethanol and 0.16 g (3.2 millimoles) of hydrazine hydrate are refluxed for 6 hours. After filtering off the product at 10° C. and drying it under reduced pressure at 50° C., 0.35 g (60% of theory) of 2-(m-aminophenyl)-3,4-diaza-bicyclo[4.1.0]hept-2-en-5-one are isolated as colorless crystals, which are identical with the compound from Example 33.
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